A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3341931



Internal ID14842199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118339027..118340725hg38UCSC Ensembl
Innerchr11:118339725..118340027hg38UCSC Ensembl
Outerchr11:118338027..118341725hg38UCSC Ensembl
chr11:118209742..118211440hg19UCSC Ensembl
Innerchr11:118210440..118210742hg19UCSC Ensembl
Outerchr11:118208742..118212440hg19UCSC Ensembl
chr11:117714952..117716650hg18UCSC Ensembl
Innerchr11:117715952..117715650hg18UCSC Ensembl
Outerchr11:117713952..117717650hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688179
SamplesNA19239
Known GenesCD3D
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3341931
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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